Cystic fibrosis has no known cure. There are treatment choices to help ease the symptoms of the disease and give the cystic fibrosis patient a better quality of life. There is no way to prevent cystic fibrosis. It is a genetic disease caused by...
The only way a person can inherit the cystic fibrosis if both their parents are carrier of the mutant cystic fibrosis gene. Scientists know that one in every thirty people are carriers of this mutant gene. Your risk is higher if you are a Caucasian...
Symptoms of cystic fibrosis will normally show in children by the age of three. Adults can be diagnosed with cystic fibrosis but that is usually rare. Each child may experience symptoms differently and some will have mild symptoms and others may be more serious. Most...
Cystic fibrosis is a disorder that causes severe lung damage and digestive problems that could result in malnutrition. The disease is inherited when both parents carry a recessive mutant gene. A child cannot inherit cystic fibrosis if only one parent carries the mutant gene....
Most patients with cystic fibrosis are diagnosed when they are infants or toddlers. Some adults may be diagnosed with the disease but this is normally rare. Modern medicine has found ways of giving a cystic fibrosis patient a better standard of living and a longer...
There is no known cure for cystic fibrosis so the main purpose of treatment is to reduce the severity of the symptoms and give the patient the best possible quality of life. New antibiotics developed recently are more effective in fighting infections and...
Cystic fibrosis symptoms are caused by heavy, thick, mucus. They include frequent coughing that brings up thick discolored mucus and frequent bouts of chest congestion and frequent pneumonia. The skin may taste salty to when the child is kissed and dehydration. The...
Often if a parents know they are both carriers of the recessive CF gene they will have undergone DNA testing and realize there is a chance their child will have cystic fibrosis. Testing can be done before the baby is born to...
Most patients with cystic fibrosis will be placed on a regular regiment of drug treatment. The gene that is known as CFTR alters the function of the protein that scatters the salt and water through the body. In normal people, this mucus is...
Scientists and researchers recently released a study showing a decline in birthrates of babies with cystic fibrosis since genetic testing became available. The general public has more knowledge and understanding of the disease that was a mystery for so long. In medieval times...
